Osteopontin is involved in migration of eosinophils in asthma

Summary Background Osteopontin (OPN) is an extracellular matrix protein with a wide range of functions, and is involved in various inflammatory diseases. However, the role of OPN in eosinophilic airway inflammation is unclear. Objective To elucidate the role of OPN in eosinophilic airway inflammatio...

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Published inClinical and experimental allergy Vol. 39; no. 8; pp. 1152 - 1159
Main Authors Takahashi, A., Kurokawa, M., Konno, S., Ito, K., Kon, S., Ashino, S., Nishimura, T., Uede, T., Hizawa, N., Huang, S-K, Nishimura, M.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.08.2009
Blackwell
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Summary:Summary Background Osteopontin (OPN) is an extracellular matrix protein with a wide range of functions, and is involved in various inflammatory diseases. However, the role of OPN in eosinophilic airway inflammation is unclear. Objective To elucidate the role of OPN in eosinophilic airway inflammation. Methods OPN protein levels in induced sputum from asthmatic patients and healthy controls were measured. Eosinophil migration assays were performed in the presence or absence of OPN, a blocking antibody (Ab) recognizing its integrin‐binding domain (2K1) and an anti‐integrin α4 Ab (P1H4). In the mouse asthma model, the levels of eosinophilia were examined in bronchoalveolar lavage fluids (BALFs) from ovalbumin (OVA)‐sensitized and ‐challenged mice with or without administration of an Ab (M5) corresponding to human 2K1. Results Levels of OPN in induced sputum were significantly higher in asthmatic patients when compared with healthy controls. In addition, levels of OPN were correlated with the percentage of sputum eosinophils. OPN induced significant migration of human eosinophils and this effect was inhibited by 2K1 and P1H4. M5 significantly attenuated OVA‐induced eosinophilia in BALFs. Conclusion These results indicate that OPN plays a role in the migration of eosinophils into the airways and may be involved in the pathogenesis of asthma.
Bibliography:istex:81D1A423D2B8654ABD1029BA5BC2E8E1A51F34AC
ark:/67375/WNG-LD67P5Q9-5
ArticleID:CEA3249
Contributed equally to this work.
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ISSN:0954-7894
1365-2222
DOI:10.1111/j.1365-2222.2009.03249.x